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Biophys J, August 2001, p. 960-968, Vol. 81, No. 2

and
*Laboratory of Biochemistry, National Heart, Lung, and Blood
Institute, and
Division of Bioengineering and Physical
Sciences, National Institutes of Health, Bethesda, Maryland 20892, and
Department of Surgery, Section of Plastic and
Reconstructive Surgery, University of Chicago, Chicago, Illinois 60637 USA
An externally applied electric field across vesicles
leads to transient perforation of the membrane. The distribution and lifetime of these pores was examined using
1,2-di-oleoyl-sn-glycero-3-phosphocholine (DOPC)
phospholipid vesicles using a standard fluorescent microscope. The
vesicle membrane was stained with a fluorescent membrane dye, and upon
field application, a single membrane pore as large as ~7 µm in
diameter was observed at the vesicle membrane facing the negative
electrode. At the anode-facing hemisphere, large and visible pores are
seldom found, but formation of many small pores is implicated by the
data. Analysis of pre- and post-field fluorescent vesicle images, as
well as images from negatively stained electron micrographs, indicate
that pore formation is associated with a partial loss of the
phospholipid bilayer from the vesicle membrane. Up to ~14% of the
membrane surface could be lost due to pore formation. Interestingly,
despite a clear difference in the size distribution of the pores
observed, the effective porous areas at both hemispheres was
approximately equal. Ca2+ influx measurements into
perforated vesicles further showed that pores are essentially resealed
within ~165 ms after the pulse. The pore distribution found in this
study is in line with an earlier hypothesis (E. Tekle, R. D. Astumian, and P. B. Chock, 1994, Proc. Natl. Acad. Sci.
U.S.A. 91:11512-11516) of asymmetric pore distribution based
on selective transport of various fluorescent markers across electroporated membranes.
Biophys J, August 2001, p. 960-968, Vol. 81, No. 2
© 2001 by the Biophysical Society 0006-3495/01/08/960/09 $2.00
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